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临床试验/NCT04880954
NCT04880954Unknown不适用

Soft Tissue Mobilization and Rehabilitation on Pain and Physical Functioning for Non-Specific Chronic Knee Pain: A Randomized Clinical Trail

Neuro Performance Integration2 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2021年3月31日最近更新:
适应症

试验速览

阶段
不适用
入组人数
36
试验地点
2
主要终点
Change in Perceived Pain

研究概览

简要总结

This is a research study examining if hands-on therapy and prescribed exercise is an effective way to manage and reduce knee pain. It will also look at physical benefits of this treatment including balance, strength, and flexibility.

Participation will include 2 assessment days and a 12-week treatment cycle. Assessments will be conducted during week 1 and after treatment. The treatment will vary based on the assigned group. This may include 12 in-person manual therapy sessions occurring once per week and or 12-weeks of at-home therapy occurring 5 times per week.

The greatest risk of participation includes possible muscle/joint soreness, injury during at-home exercises, and loss of confidentiality.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

盲法说明

Participants will know the group they are randomly assigned.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults experiencing non-specific knee pain for 3 or more months. Pain must be 3/10 (VAS) or higher.

排除标准

  • Pain due to knee surgery, fracture, tumor, trauma, or those on medication for mood disorder (assessed on case by case basis).

结局指标

主要结局

Change in Perceived Pain

时间窗: This will be measured pre- and post- intervention (week 1 and week 13).

The Visual Analogue Scale (VAS) will be used to quantify pain. The scale ranges from 1 (no pain) to 10 (worst pain).

次要结局

  • Modified Clinical Test of Sensory Integration and Balance(This will be measured pre- and post- intervention (week 1 and week 13).)
  • Isometric Strength(This will be measured pre- and post- intervention (week 1 and week 13).)
  • Range of Motion(This will be measured pre- and post- intervention (week 1 and week 13))
  • Limits of Stability(This will be measured pre- and post- intervention (week 1 and week 13).)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Beverly Albert

Research Director

Neuro Performance Integration

研究点 (2)

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